Tomato line FDR-9Q10189

ABSTRACT

The invention provides seed and plants of tomato line FDR-9Q10189. The invention thus relates to the plants, seeds and tissue cultures of tomato line FDR-9Q10189, and to methods for producing a tomato plant produced by crossing such plants with themselves or with another tomato plant, such as a plant of another genotype. The invention further relates to seeds and plants produced by such crossing. The invention further relates to parts of such plants, including the fruit and gametes of such plants.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No.15/693,346, filed Aug. 31, 2017, the entire disclosure of which isincorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to the field of plant breeding and, morespecifically, to the development of tomato hybrid SVTD0140 and theinbred tomato lines FDR9Q14-0260 and FDR-9Q10189.

BACKGROUND OF THE INVENTION

The goal of vegetable breeding is to combine various desirable traits ina single variety/hybrid. Such desirable traits may include any traitdeemed beneficial by a grower and/or consumer, including greater yield,resistance to insects and pathogens, tolerance to environmental stress,and nutritional value.

Breeding techniques take advantage of a plant's method of pollination.There are two general methods of pollination: a plant self-pollinates ifpollen from one flower is transferred to the same or another flower ofthe same plant or plant variety. A plant cross-pollinates if pollencomes to it from a flower of a different plant variety.

Plants that have been self-pollinated and selected for type over manygenerations become homozygous at almost all gene loci and produce auniform population of true breeding progeny, a homozygous plant. A crossbetween two such homozygous plants of different genotypes produces auniform population of hybrid plants that are heterozygous for many geneloci. Conversely, a cross of two plants each heterozygous at a number ofloci produces a population of hybrid plants that differ genetically andare not uniform. The resulting non-uniformity makes performanceunpredictable.

The development of uniform varieties requires the development ofhomozygous inbred plants, the crossing of these inbred plants, and theevaluation of the crosses. Pedigree breeding and recurrent selection areexamples of breeding methods that have been used to develop inbredplants from breeding populations. Those breeding methods combine thegenetic backgrounds from two or more plants or various other broad-basedsources into breeding pools from which new lines and hybrids derivedtherefrom are developed by selfing and selection of desired phenotypes.The new lines and hybrids are evaluated to determine which of those havecommercial potential.

SUMMARY OF THE INVENTION

In one aspect, the present invention provides a tomato plant of thehybrid designated SVTD0140, the tomato line FDR9Q14-0260 or tomato lineFDR-9Q10189. Also provided are tomato plants having all thephysiological and morphological characteristics of such a plant. Partsof these tomato plants are also provided, for example, including pollen,an ovule, scion, a rootstock, a fruit, and a cell of the plant.

In another aspect of the invention, a plant of tomato hybrid SVTD0140and/or tomato lines FDR9Q14-0260 and FDR-9Q10189 comprising an addedheritable trait is provided. The heritable trait may comprise a geneticlocus that is, for example, a dominant or recessive allele. In oneembodiment of the invention, a plant of tomato hybrid SVTD0140 and/ortomato lines FDR9Q14-0260 and FDR-9Q10189 is defined as comprising asingle locus conversion. In specific embodiments of the invention, anadded genetic locus confers one or more traits such as, for example,herbicide tolerance, insect resistance, disease resistance, and modifiedcarbohydrate metabolism. In further embodiments, the trait may beconferred by a naturally occurring gene introduced into the genome of aline by backcrossing, a natural or induced mutation, or a transgeneintroduced through genetic transformation techniques into the plant or aprogenitor of any previous generation thereof. When introduced throughtransformation, a genetic locus may comprise one or more genesintegrated at a single chromosomal location.

The invention also concerns the seed of tomato hybrid SVTD0140 and/ortomato lines FDR9Q14-0260 and FDR-9Q10189. The tomato seed of theinvention may be provided as an essentially homogeneous population oftomato seed of tomato hybrid SVTD0140 and/or tomato lines FDR9Q14-0260and FDR-9Q10189. Essentially homogeneous populations of seed aregenerally free from substantial numbers of other seed. Therefore, insome embodiments, seed of hybrid SVTD0140 and/or tomato linesFDR9Q14-0260 and FDR-9Q10189 may be defined as forming at least about97% of the total seed, including at least about 98%, 99% or more of theseed. The seed population may be separately grown to provide anessentially homogeneous population of tomato plants designated SVTD0140and/or tomato lines FDR9Q14-0260 and FDR-9Q10189.

In yet another aspect of the invention, a tissue culture of regenerablecells of a tomato plant of hybrid SVTD0140 and/or tomato linesFDR9Q14-0260 and FDR-9Q10189 is provided. The tissue culture willpreferably be capable of regenerating tomato plants capable ofexpressing all of the physiological and morphological characteristics ofthe starting plant, and of regenerating plants having substantially thesame genotype as the starting plant. Examples of some of thephysiological and morphological characteristics of the hybrid SVTD0140and/or tomato lines FDR9Q14-0260 and FDR-9Q10189 include those traitsset forth in the tables herein. The regenerable cells in such tissuecultures may be derived, for example, from embryos, meristems,cotyledons, pollen, leaves, anthers, roots, root tips, pistils, flowers,seed and stalks. Still further, the present invention provides tomatoplants regenerated from a tissue culture of the invention, the plantshaving all the physiological and morphological characteristics of hybridSVTD0140 and/or tomato lines FDR9Q14-0260 and FDR-9Q10189.

In still yet another aspect of the invention, processes are provided forproducing tomato seeds, plants and fruit, which processes generallycomprise crossing a first parent tomato plant with a second parenttomato plant, wherein at least one of the first or second parent tomatoplants is a plant of tomato line FDR9Q14-0260 or tomato lineFDR-9Q10189. These processes may be further exemplified as processes forpreparing hybrid tomato seed or plants, wherein a first tomato plant iscrossed with a second tomato plant of a different, distinct genotype toprovide a hybrid that has, as one of its parents, a plant of tomato lineFDR9Q14-0260 or tomato line FDR-9Q10189. In these processes, crossingwill result in the production of seed. The seed production occursregardless of whether the seed is collected or not.

In one embodiment of the invention, the first step in “crossing”comprises planting seeds of a first and second parent tomato plant,often in proximity so that pollination will occur for example, mediatedby insect vectors. Alternatively, pollen can be transferred manually.Where the plant is self-pollinated, pollination may occur without theneed for direct human intervention other than plant cultivation.

A second step may comprise cultivating or growing the seeds of first andsecond parent tomato plants into plants that bear flowers. A third stepmay comprise preventing self-pollination of the plants, such as byemasculating the flowers (i.e., killing or removing the pollen).

A fourth step for a hybrid cross may comprise cross-pollination betweenthe first and second parent tomato plants. Yet another step comprisesharvesting the seeds from at least one of the parent tomato plants. Theharvested seed can be grown to produce a tomato plant or hybrid tomatoplant.

The present invention also provides the tomato seeds and plants producedby a process that comprises crossing a first parent tomato plant with asecond parent tomato plant, wherein at least one of the first or secondparent tomato plants is a plant of tomato hybrid SVTD0140 and/or tomatolines FDR9Q14-0260 and FDR-9Q10189. In one embodiment of the invention,tomato seed and plants produced by the process are first generation (F₁)hybrid tomato seed and plants produced by crossing a plant in accordancewith the invention with another, distinct plant. The present inventionfurther contemplates plant parts of such an F₁ hybrid tomato plant, andmethods of use thereof. Therefore, certain exemplary embodiments of theinvention provide an F₁ hybrid tomato plant and seed thereof.

In still yet another aspect, the present invention provides a method ofproducing a plant derived from hybrid SVTD0140 and/or tomato linesFDR9Q14-0260 and FDR-9Q10189, the method comprising the steps of: (a)preparing a progeny plant derived from hybrid SVTD0140 and/or tomatolines FDR9Q14-0260 and FDR-9Q10189, wherein said preparing comprisescrossing a plant of the hybrid SVTD0140 and/or tomato lines FDR9Q14-0260and FDR-9Q10189 with a second plant; and (b) crossing the progeny plantwith itself or a second plant to produce a seed of a progeny plant of asubsequent generation. In further embodiments, the method mayadditionally comprise: (c) growing a progeny plant of a subsequentgeneration from said seed of a progeny plant of a subsequent generationand crossing the progeny plant of a subsequent generation with itself ora second plant; and repeating the steps for an additional 3-10generations to produce a plant derived from hybrid SVTD0140 and/ortomato lines FDR9Q14-0260 and FDR-9Q10189. The plant derived from hybridSVTD0140 and/or tomato lines FDR9Q14-0260 and FDR-9Q10189 may be aninbred line, and the aforementioned repeated crossing steps may bedefined as comprising sufficient inbreeding to produce the inbred line.In the method, it may be desirable to select particular plants resultingfrom step (c) for continued crossing according to steps (b) and (c). Byselecting plants having one or more desirable traits, a plant derivedfrom hybrid SVTD0140 and/or tomato lines FDR9Q14-0260 and FDR-9Q10189 isobtained which possesses some of the desirable traits of the line/hybridas well as potentially other selected traits.

In certain embodiments, the present invention provides a method ofproducing food or feed comprising: (a) obtaining a plant of tomatohybrid SVTD0140 and/or tomato lines FDR9Q14-0260 and FDR-9Q10189,wherein the plant has been cultivated to maturity, and (b) collecting atleast one tomato from the plant.

In still yet another aspect of the invention, the genetic complement oftomato hybrid SVTD0140 and/or tomato lines FDR9Q14-0260 and FDR-9Q10189is provided. The phrase “genetic complement” is used to refer to theaggregate of nucleotide sequences, the expression of which sequencesdefines the phenotype of, in the present case, a tomato plant, or a cellor tissue of that plant. A genetic complement thus represents thegenetic makeup of a cell, tissue or plant, and a hybrid geneticcomplement represents the genetic make-up of a hybrid cell, tissue orplant. The invention thus provides tomato plant cells that have agenetic complement in accordance with the tomato plant cells disclosedherein, and seeds and plants containing such cells.

Plant genetic complements may be assessed by genetic marker profiles,and by the expression of phenotypic traits that are characteristic ofthe expression of the genetic complement, e.g., isozyme typing profiles.It is understood that hybrid SVTD0140 and/or tomato lines FDR9Q14-0260and FDR-9Q10189 could be identified by any of the many well-knowntechniques such as, for example, Simple Sequence Length Polymorphisms(SSLPs) (Williams et al., Nucleic Acids Res., 1 8:6531-6535, 1990),Randomly Amplified Polymorphic DNAs (RAPDs), DNA AmplificationFingerprinting (DAF), Sequence Characterized Amplified Regions (SCARs),Arbitrary Primed Polymerase Chain Reaction (AP-PCR), Amplified FragmentLength Polymorphisms (AFLPs) (EP 534 858, specifically incorporatedherein by reference in its entirety), and Single NucleotidePolymorphisms (SNPs) (Wang et al., Science, 280:1077-1082, 1998).

In still yet another aspect, the present invention provides hybridgenetic complements, as represented by tomato plant cells, tissues,plants, and seeds, formed by the combination of a haploid geneticcomplement of a tomato plant of the invention with a haploid geneticcomplement of a second tomato plant, preferably, another, distincttomato plant. In another aspect, the present invention provides a tomatoplant regenerated from a tissue culture that comprises a hybrid geneticcomplement of this invention.

Any embodiment discussed herein with respect to one aspect of theinvention applies to other aspects of the invention as well, unlessspecifically noted.

The term “about” is used to indicate that a value includes the standarddeviation of the mean for the device or method being employed todetermine the value. The use of the term “or” in the claims is used tomean “and/or” unless explicitly indicated to refer to alternatives onlyor the alternatives are mutually exclusive. When used in conjunctionwith the word “comprising” or other open language in the claims, thewords “a” and “an” denote “one or more,” unless specifically notedotherwise. The terms “comprise,” “have” and “include” are open-endedlinking verbs. Any forms or tenses of one or more of these verbs, suchas “comprises,” “comprising,” “has,” “having,” “includes” and“including,” are also open-ended. For example, any method that“comprises,” “has” or “includes” one or more steps is not limited topossessing only those one or more steps and also covers other unlistedsteps. Similarly, any plant that “comprises,” “has” or “includes” one ormore traits is not limited to possessing only those one or more traitsand covers other unlisted traits.

Other objects, features, and advantages of the present invention willbecome apparent from the following detailed description. It should beunderstood, however, that the detailed description and any specificexamples provided, while indicating specific embodiments of theinvention, are given by way of illustration only, since various changesand modifications within the spirit and scope of the invention willbecome apparent to those skilled in the art from this detaileddescription.

DETAILED DESCRIPTION OF THE INVENTION

The invention provides methods and compositions relating to plants,seeds and derivatives of tomato hybrid SVTD0140, tomato lineFDR9Q14-0260, and tomato line FDR-9Q10189.

Tomato hybrid SVTD0140, also known as 12-9Q-FDR-2615, is determinate,round variety intended for the fresh market that is widely adapted togrowing conditions in the southeastern United States. Hybrid SVTD0140comprises a strong plant type with good fruit cover and a highpercentage of extra-large fruit of good quality. Hybrid SVTD0140comprises resistance to Alternaria alternata f. sp. lycopersici (Aal),Fusarium oxysporum f. sp. lycopersici U.S. Races 1-3 (Fo10, Fol1, Fol2),Fusarium oxysporum f. sp. radicis-lycopersici (For), Tomato spotted wiltvirus (TSWV), Stemphylium solani (Ss), and Verticilliumdahliae/Verticillium albo-atrum U.S. Race 1 (Va/Vd). Hybrid SVTD0140provides added resistance to Fusarium oxysporum f. sp. lycopersici U.S.Races 1-3 (Fol0, Fol1, Fol2), Fusarium oxysporum f. sp.radicis-lycopersici (For), and Tomato spotted wilt virus (TSWV) whencompared to commercial variety Florida 47R and provides added resistanceto Tomato spotted wilt virus (TSWV) and higher fruit quality whencompared to commercial variety Soraya.

Tomato line FDR9Q14-0260 is an inbred variety that develops a largeplant with good cover that produces a heavy set of smooth, firm,flattened oblate, extra-large, maturing to red fruit with a jointedpedicel and uniform green shoulders. Line FDR9Q14-0260 comprisesresistance to Meloidogyne incognita (Mi), Meloidogyne arenaria (Ma),Meloidogyne javanica (Mj), Tomato spotted wilt virus (TSWV), Alternariaalternata f. sp. lycopersici (Aal), Stemphylium solani (Ss), Fusariumoxysporum f. sp. lycopersici U.S. Races 1, 2 (Fol1, Fol2), andVerticillium dahliae/Verticillium albo-atrum U.S. Race 1 (Va/Vd).

Tomato line FDR-9Q10189 is an inbred variety that develops a mediumplant with light cover that produces a heavy set of smooth, firm, deepoblate, large, maturing to red fruit with a jointed pedicel and uniformgreen shoulders. Line FDR-9Q10189 comprises resistance to Fusariumoxysporum f. sp. radicis-lycopersici (For), Fusarium oxysporum f. sp.lycopersici U.S. Races 3 (Fol2), Alternaria alternata f. sp. lycopersici(Aal), Fusarium oxysporum f. sp. lycopersici U.S. Races 1, 2 (Fol0,Fol1), Stemphylium solani (Ss), and Verticillium dahliae/Verticilliumalbo-atrum U.S. Race 1 (Va/Vd).

A. Origin and Breeding History of Tomato Hybrid SVTD0140

The parents of hybrid SVTD0140 are FDR9Q14-0260 and FDR-9Q10189. Theparent lines are uniform and stable, as is a hybrid produced therefrom.A small percentage of variants can occur within commercially acceptablelimits for almost any characteristic during the course of repeatedmultiplication. However no variants are expected.

B. Physiological and Morphological Characteristics of Tomato HybridSVTD0140, Tomato Line FDR9Q14-0260, and Tomato Line FDR-9Q10189

In accordance with one aspect of the present invention, there isprovided a plant having the physiological and morphologicalcharacteristics of tomato hybrid SVTD0140 and the parent lines thereof.A description of the physiological and morphological characteristics ofsuch plants is presented in Tables 1-3.

TABLE 1 Physiological and Morphological Characteristics of Tomato HybridSVTD0140 CHARACTERISTIC SVTD0140 Florida 47 1. Seedling anthocyanin inhypocotyl of 2-15 cm present present seedling habit of 3-4 week oldseedling normal normal 2. Mature Plant height 61.13 cm 59.93 cm growthtype determinate determinate form normal compact size of canopy(compared to others of medium medium similar type) habit sprawlingsemi-erect 3. Stem branching intermediate intermediate branching atcotyledon or first leafy present absent node number of nodes betweenfirst  7 to 10 4 to 7 inflorescence number of nodes between early (firstto 1 to 4 1 to 4 second, second to third) inflorescences number of nodesbetween later 1 to 4 1 to 4 developing inflorescences pubescence onyounger stems moderately hairy moderately hairy 4. Leaf type (matureleaf beneath the third tomato tomato inflorescence) margins of majorleaflets (mature leaf shallowly toothed or deeply toothed or cut,beneath the third inflorescence) scalloped sps. toward base marginalrolling or wiltiness (mature moderate strong leaf beneath the thirdinflorescence) onset of leaflet rolling (mature leaf mid-seasonmid-season beneath the third inflorescence) surface of major leaflets(mature leaf rugose rugose beneath the third inflorescence) (bumpy orveiny) (bumpy or veiny) pubescence (mature leaf beneath the normalsmooth third inflorescence) (no long hairs) 5. Inflorescence type (thirdinflorescence) simple forked (2 major axes) average number of flowers in4.6 5.4 inflorescence (third inflorescence) leafy or “running”inflorescence (third occasional absent inflorescence) 6. Flower calyxnormal normal (lobes awl shaped) (lobes awl shaped) calyx-lobes shorterthan corolla shorter than corolla corolla color yellow yellow stylepubescence sparse sparse anthers all fused into tube all fused into tubefasciation (first flower of second or third absent absent inflorescence)abscission layer present present (pedicellate) (pedicellate) 7. Fruitsurface smooth smooth base color (mature-green stage) light gray-greenlight green pattern (mature-green stage) uniform green uniform greenshape of transverse section (third fruit of irregular flattened secondor third cluster) shape of blossom end (third fruit of indented flatsecond or third cluster) shape of stem end (third fruit of secondindented indented or third cluster) shape of pistil scar (third fruit ofsecond stellate stellate or third cluster) point of detachment of fruitat harvest at pedicel joint at calyx attachment (third fruit of secondor third cluster) stem scar size medium medium length of pedicel (thirdfruit of second 12.62 mm 13.12 mm or third cluster) length of maturefruit (stem axis) 64.44 mm 59.62 mm Check Variety Rutgers diameter offruit at widest point 79.70 mm 67.62 mm Check Variety Rutgers weight ofmature fruit 243.6 g 159.73 g Check Variety Rutgers core present presentnumber of locules five or more five or more color, full ripe red redflesh color, full-ripe red/crimson red/crimson flesh color with lighteror darker with lighter or darker areas in walls areas in walls loculargel color of table-ripe fruit red red ripening blossom-to-stem enduniform epidermis color yellow yellow epidermis easy-peel normalepidermis texture tender tender thickness of pericarp 6.63 mm 6.70 mmCheck Variety Rutgers 8. Phenology seeding to 50% flow (one open on 50%63 days 65 days of plants) seeding to once over harvest 119 days 120days fruiting season long medium 9. Adaptation culture field field 10.Chemistry and Composition of Full-Ripe Fruits pH 4.2 4.1 titratableacidity, as % citric 0.4 0.561 total solids (dry matter, seeds, and skin5.5 6.4 removed) soluble solids, as °Bx 4.8 5.9

-   These are typical values. Values may vary due to environment. Other    values that are substantially equivalent are within the scope of the    invention.

TABLE 2 Physiological and Morphological Characteristics of Tomato LineFDR9Q14-0260 CHARACTERISTIC FDR9Q14-0260 Florida 47 1. Seedlinganthocyanin in hypocotyl of 2-15 cm present present seedling habit of3-4 week old seedling normal normal 2. Mature Plant height 53 cm 59.93cm growth type determinate determinate form compact compact size ofcanopy (compared to others of small medium similar type) habit sprawlingsemi-erect 3. Stem branching intermediate intermediate branching atcotyledon or first leafy absent absent node number of nodes betweenfirst  7 to 10 4 to 7 inflorescence number of nodes between early (firstto 1 to 4 1 to 4 second, second to third) inflorescences number of nodesbetween later 1 to 4 1 to 4 developing inflorescences pubescence onyounger stems moderately hairy moderately hairy 4. Leaf type (matureleaf beneath the third tomato tomato inflorescence) margins of majorleaflets (mature leaf deeply toothed or cut, deeply toothed or cut,beneath the third inflorescence) sps. toward base sps. toward basemarginal rolling or wiltiness (mature strong strong leaf beneath thethird inflorescence) onset of leaflet rolling (mature leaf mid-seasonmid-season beneath the third inflorescence) surface of major leaflets(mature leaf rugose rugose beneath the third inflorescence) (bumpy orveiny) (bumpy or veiny) pubescence (mature leaf beneath the smoothsmooth third inflorescence) (no long hairs) (no long hairs) 5.Inflorescence type (third inflorescence) simple forked (2 major axes)average number of flowers in 6.13 5.4 inflorescence (thirdinflorescence) leafy or “running” inflorescence (third absent absentinflorescence) 6. Flower calyx normal normal (lobes awl shaped) (lobesawl shaped) calyx-lobes approximately shorter than corolla equalingcorolla corolla color yellow yellow style pubescence absent sparseanthers all fused into tube all fused into tube fasciation (first flowerof second or third absent absent inflorescence) abscission layer presentpresent (pedicellate) (pedicellate) 7. Fruit surface smooth smooth basecolor (mature-green stage) apple or medium green light green pattern(mature-green stage) uniform green uniform green shape of transversesection (third fruit of irregular flattened second or third cluster)shape of blossom end (third fruit of indented flat second or thirdcluster) shape of stem end (third fruit of second indented indented orthird cluster) shape of pistil scar (third fruit of second irregularstellate or third cluster) point of detachment of fruit at harvest atcalyx attachment at calyx attachment (third fruit of second or thirdcluster) stem scar size medium medium length of pedicel (third fruit ofsecond 15.56 mm 13.12 mm or third cluster) length of mature fruit (stemaxis) 61.6 mm 59.62 mm Check Variety Rutgers diameter of fruit at widestpoint 74.33 mm 67.62 mm Check Variety Rutgers weight of mature fruit 221g 159.73 g Check Variety Rutgers core present present number of loculesfive or more five or more color, full ripe red red flesh color,full-ripe red/crimson red/crimson flesh color with lighter or darkerwith lighter or darker areas in walls areas in walls locular gel colorof table-ripe fruit red red ripening blossom-to-stem end uniformepidermis color yellow yellow epidermis normal normal epidermis textureaverage tender thickness of pericarp 6.36 mm 6.70 mm Check VarietyRutgers 8. Phenology seeding to 50% flow (one open on 50% 64 days 65days of plants) seeding to once over harvest 119 days 120 days fruitingseason long medium 9. Adaptation culture field field 10. Chemistry andComposition of Full-Ripe Fruits pH 4.1 4.1 titratable acidity, as %citric 0.536 0.561 total solids (dry matter, seeds, and skin 6.9 6.4removed) soluble solids, as °Bx 6.2 5.9

-   These are typical values. Values may vary due to environment. Other    values that are substantially equivalent are within the scope of the    invention.

TABLE 3 Physiological and Morphological Characteristics of Tomato LineFDR-9Q10189 CHARACTERISTIC FDR-9Q10189 Florida 47 1. Seedlinganthocyanin in hypocotyl of 2-15 cm present present seedling habit of3-4 week old seedling normal normal 2. Mature Plant height 57.33 cm69.06 cm growth type determinate determinate number of inflorescences onmain stem medium few (side shoots to be removed) form normal normal sizeof canopy (compared to others of medium large similar type) habitsemi-erect semi-erect 3. Stem anthocyanin coloration absent or very weakabsent or very weak branching intermediate profuse branching atcotyledon or first leafy present absent node number of nodes betweenfirst 4 to 7 4 to 7 inflorescence number of nodes between early (firstto 4 to 7 4 to 7 second, second to third) inflorescences number of nodesbetween later 1 to 4 1 to 4 developing inflorescences pubescence onyounger stems moderately hairy moderately hairy 4. Leaf type (matureleaf beneath the third tomato tomato inflorescence) type of bladebipinnate bipinnate margins of major leaflets (mature leaf shallowlytoothed or deeply toothed or cut, beneath the third inflorescence)scalloped sps. toward base marginal rolling or wiltiness (maturemoderate moderate leaf beneath the third inflorescence) onset of leafletrolling (mature leaf mid-season mid-season beneath the thirdinflorescence) surface of major leaflets (mature leaf rugose rugosebeneath the third inflorescence) (bumpy or veiny) (bumpy or veiny)pubescence (mature leaf beneath the hirsute normal third inflorescence)5. Inflorescence attitude semi-erect semi-erect length medium long widthnarrow broad size of leaflets small large intensity of green color darkdark glossiness strong strong blistering strong strong attitude ofpetiole of leaflet in relation to semi-drooping semi-erect main axisinflorescence type mainly uniparous mainly uniparous inflorescence type(third inflorescence) simple simple average number of flowers in 4.464.6 inflorescence (third inflorescence) leafy or “running” inflorescence(third occasional occasional inflorescence) 6. Flower color yellowyellow calyx normal normal (lobes awl shaped) (lobes awl shaped)calyx-lobes approximately approximately equaling corolla equalingcorolla corolla color yellow yellow style pubescence sparse sparseanthers all fused into tube all fused into tube fasciation (first flowerof second or third absent absent inflorescence) abscission layer presentpresent (pedicellate) (pedicellate) pedicel length medium medium 7.Fruit surface smooth smooth base color (mature-green stage) light greenapple or medium green pattern (mature-green stage) uniform green uniformgreen green shoulder (before maturity) absent absent intensity of greencolor excluding light medium shoulder (before maturity) green stripes(before maturity) absent absent size large large ratio length/diametermedium medium shape in longitudinal section cordate circular shape oftransverse/cross section (third angular round fruit of second or thirdcluster) shape of stem end (third fruit of second flat flat or thirdcluster) shape of blossom end flat to pointed flat shape of pistil scar(third fruit of second stellate irregular or third cluster) ribbing atpeduncle end absent or very weak weak depression at peduncle end weakweak size of stem/peduncle scar large very large size of blossom scarsmall small point of detachment of fruit at harvest at pedicel joint atpedicel joint (third fruit of second or third cluster) length of pedicel(from joint to calyx 25.07 mm 13.17 mm attachment) length of maturefruit (stem axis) 72.86 mm 68.79 mm Check Variety Rutgers diameter offruit at widest point 75.48 mm 77.26 mm Check Variety Rutgers weight ofmature fruit 216.86 g 225.46 g Check Variety Rutgers core presentpresent diameter of core in cross section in large large relation tototal diameter number of locules more than six four, five, or six color,full ripe red red color (at maturity) red red flesh color, full-ripered/crimson red/crimson color of flesh (at maturity) red red glossinessof skin medium medium flesh color with lighter or darker with lighter ordarker areas in walls areas in walls locular gel color of table-ripefruit red red firmness soft soft shelf life short very short time offlowering medium medium time of maturity medium medium ripening uniformuniform epidermis color yellow yellow epidermis easy-peel easy-peelepidermis texture tender tender thickness of pericarp 7.64 mm 6.35 mmCheck Variety Rutgers thickness of pericarp thick thick sensitivity tosilvering insensitive insensitive 8. Phenology seeding to 50% flow (oneopen on 50% 67 days 66 days of plants) seeding to once over harvest 121days 122 days 9. Adaptation culture field field 10. Chemistry andComposition of Full-Ripe Fruits pH 4.3 4.3 titratable acidity, as %citric 0.31 0.38 total solids (dry matter, seeds, and skin 5 4.8removed) soluble solids, as °Bx 4.6 4.2

-   These are typical values. Values may vary due to environment. Other    values that are substantially equivalent are within the scope of the    invention.

C. Breeding Tomato Plants

One aspect of the current invention concerns methods for producing seedof tomato hybrid SVTD0140 involving crossing tomato lines FDR9Q14-0260and FDR-9Q10189. Alternatively, in other embodiments of the invention,hybrid SVTD0140, line FDR9Q14-0260, or line FDR-9Q10189 may be crossedwith itself or with any second plant. Such methods can be used forpropagation of hybrid SVTD0140 and/or the tomato lines FDR9Q14-0260 andFDR-9Q10189, or can be used to produce plants that are derived fromhybrid SVTD0140 and/or the tomato lines FDR9Q14-0260 and FDR-9Q10189.Plants derived from hybrid SVTD0140 and/or the tomato lines FDR9Q14-0260and FDR-9Q10189 may be used, in certain embodiments, for the developmentof new tomato varieties.

The development of new varieties using one or more starting varieties iswell known in the art. In accordance with the invention, novel varietiesmay be created by crossing hybrid SVTD0140 followed by multiplegenerations of breeding according to such well-known methods. Newvarieties may be created by crossing with any second plant. In selectingsuch a second plant to cross for the purpose of developing novel lines,it may be desired to choose those plants which either themselves exhibitone or more selected desirable characteristics or which exhibit thedesired characteristic(s) when in hybrid combination. Once initialcrosses have been made, inbreeding and selection take place to producenew varieties. For development of a uniform line, often five or moregenerations of selfing and selection are involved.

Uniform lines of new varieties may also be developed by way ofdouble-haploids. This technique allows the creation of true breedinglines without the need for multiple generations of selfing andselection. In this manner true breeding lines can be produced in aslittle as one generation. Haploid embryos may be produced frommicrospores, pollen, anther cultures, or ovary cultures. The haploidembryos may then be doubled autonomously, or by chemical treatments(e.g. colchicine treatment). Alternatively, haploid embryos may be growninto haploid plants and treated to induce chromosome doubling. In eithercase, fertile homozygous plants are obtained. In accordance with theinvention, any of such techniques may be used in connection with a plantof the invention and progeny thereof to achieve a homozygous line.

Backcrossing can also be used to improve an inbred plant. Backcrossingtransfers a specific desirable trait from one inbred or non-inbredsource to an inbred that lacks that trait. This can be accomplished, forexample, by first crossing a superior inbred (A) (recurrent parent) to adonor inbred (non-recurrent parent), which carries the appropriate locusor loci for the trait in question. The progeny of this cross are thenmated back to the superior recurrent parent (A) followed by selection inthe resultant progeny for the desired trait to be transferred from thenon-recurrent parent. After five or more backcross generations withselection for the desired trait, the progeny have the characteristicbeing transferred, but are like the superior parent for most or almostall other loci. The last backcross generation would be selfed to givepure breeding progeny for the trait being transferred.

The plants of the present invention are particularly well suited for thedevelopment of new lines based on the elite nature of the geneticbackground of the plants. In selecting a second plant to cross withSVTD0140 and/or tomato lines FDR9Q14-0260 and FDR-9Q10189 for thepurpose of developing novel tomato lines, it will typically be preferredto choose those plants which either themselves exhibit one or moreselected desirable characteristics or which exhibit the desiredcharacteristic(s) when in hybrid combination. Examples of desirabletraits may include, in specific embodiments, high seed yield, high seedgermination, seedling vigor, high fruit yield, disease tolerance orresistance, adaptability for soil and climate conditions, and delayedfruit ripening. Consumer-driven traits, such as a fruit shape, color,texture, and taste are other examples of traits that may be incorporatedinto new lines of tomato plants developed by this invention.

Delayed fruit ripening is a trait that is especially desirable in tomatoproduction, in that it provides a number of important benefits includingan increase in fruit shelf life, the ability to transport fruit longerdistances, the reduction of spoiling of fruit during transport orstorage, and an increase in the flexibility of harvest time. The abilityto delay harvest is especially useful for the processing industry astomato fruits may be picked in a single harvest. A number of genes havebeen identified as playing a role in fruit ripening in tomato. Mutationsin some of these genes were observed to be correlated with an extendedshelf life phenotype (Gang et al., Adv. Hort. Sci. 22: 54-62, 2008). Forexample, WO2010042865 discloses that certain mutations in the 2nd or 3rdexon in the non-ripening (NOR) gene can result in extended shelf lifephenotypes. These mutations are believed to result in an early stopcodon. It is therefore expected that any mutation resulting in an earlystop codon in an exon in the NOR gene, particularly a mutation resultingin an early stop codon in the 3rd exon, will result in a slower ripeningor an extended shelf life phenotype in tomato. A marker to select forthe unique mutation of each allele and to distinguish between thedifferent alleles of the NOR gene in a breeding program can be developedby methods known in the art.

D. Further Embodiments of the Invention

In certain aspects of the invention, plants described herein areprovided modified to include at least a first desired heritable trait.Such plants may, in one embodiment, be developed by a plant breedingtechnique called backcrossing, wherein essentially all of themorphological and physiological characteristics of a variety arerecovered in addition to a genetic locus transferred into the plant viathe backcrossing technique. The term single locus converted plant asused herein refers to those tomato plants which are developed by a plantbreeding technique called backcrossing, wherein essentially all of themorphological and physiological characteristics of a variety arerecovered in addition to the single locus transferred into the varietyvia the backcrossing technique. By essentially all of the morphologicaland physiological characteristics, it is meant that the characteristicsof a plant are recovered that are otherwise present when compared in thesame environment, other than an occasional variant trait that mightarise during backcrossing or direct introduction of a transgene.

Backcrossing methods can be used with the present invention to improveor introduce a characteristic into the present variety. The parentaltomato plant which contributes the locus for the desired characteristicis termed the nonrecurrent or donor parent. This terminology refers tothe fact that the nonrecurrent parent is used one time in the backcrossprotocol and therefore does not recur. The parental tomato plant towhich the locus or loci from the nonrecurrent parent are transferred isknown as the recurrent parent as it is used for several rounds in thebackcrossing protocol.

In a typical backcross protocol, the original variety of interest(recurrent parent) is crossed to a second variety (nonrecurrent parent)that carries the single locus of interest to be transferred. Theresulting progeny from this cross are then crossed again to therecurrent parent and the process is repeated until a tomato plant isobtained wherein essentially all of the morphological and physiologicalcharacteristics of the recurrent parent are recovered in the convertedplant, in addition to the single transferred locus from the nonrecurrentparent.

The selection of a suitable recurrent parent is an important step for asuccessful backcrossing procedure. The goal of a backcross protocol isto alter or substitute a single trait or characteristic in the originalvariety. To accomplish this, a single locus of the recurrent variety ismodified or substituted with the desired locus from the nonrecurrentparent, while retaining essentially all of the rest of the desiredgenetic, and therefore the desired physiological and morphologicalconstitution of the original variety. The choice of the particularnonrecurrent parent will depend on the purpose of the backcross; one ofthe major purposes is to add some commercially desirable trait to theplant. The exact backcrossing protocol will depend on the characteristicor trait being altered and the genetic distance between the recurrentand nonrecurrent parents. Although backcrossing methods are simplifiedwhen the characteristic being transferred is a dominant allele, arecessive allele, or an additive allele (between recessive anddominant), may also be transferred. In this instance it may be necessaryto introduce a test of the progeny to determine if the desiredcharacteristic has been successfully transferred.

In one embodiment, progeny tomato plants of a backcross in which a plantdescribed herein is the recurrent parent comprise (i) the desired traitfrom the non-recurrent parent and (ii) all of the physiological andmorphological characteristics of tomato the recurrent parent asdetermined at the 5% significance level when grown in the sameenvironmental conditions.

New varieties can also be developed from more than two parents. Thetechnique, known as modified backcrossing, uses different recurrentparents during the backcrossing. Modified backcrossing may be used toreplace the original recurrent parent with a variety having certain moredesirable characteristics or multiple parents may be used to obtaindifferent desirable characteristics from each.

With the development of molecular markers associated with particulartraits, it is possible to add additional traits into an established germline, such as represented here, with the end result being substantiallythe same base germplasm with the addition of a new trait or traits.Molecular breeding, as described in Moose and Mumm, 2008 (PlantPhysiol., 147: 969-977), for example, and elsewhere, provides amechanism for integrating single or multiple traits or QTL into an eliteline. This molecular breeding-facilitated movement of a trait or traitsinto an elite line may encompass incorporation of a particular genomicfragment associated with a particular trait of interest into the eliteline by the mechanism of identification of the integrated genomicfragment with the use of flanking or associated marker assays. In theembodiment represented here, one, two, three or four genomic loci, forexample, may be integrated into an elite line via this methodology. Whenthis elite line containing the additional loci is further crossed withanother parental elite line to produce hybrid offspring, it is possibleto then incorporate at least eight separate additional loci into thehybrid. These additional loci may confer, for example, such traits as adisease resistance or a fruit quality trait. In one embodiment, eachlocus may confer a separate trait. In another embodiment, loci may needto be homozygous and exist in each parent line to confer a trait in thehybrid. In yet another embodiment, multiple loci may be combined toconfer a single robust phenotype of a desired trait.

Many single locus traits have been identified that are not regularlyselected for in the development of a new inbred but that can be improvedby backcrossing techniques. Single locus traits may or may not betransgenic; examples of these traits include, but are not limited to,herbicide resistance, resistance to bacterial, fungal, or viral disease,insect resistance, modified fatty acid or carbohydrate metabolism, andaltered nutritional quality. These comprise genes generally inheritedthrough the nucleus.

Direct selection may be applied where the single locus acts as adominant trait. For this selection process, the progeny of the initialcross are assayed for viral resistance and/or the presence of thecorresponding gene prior to the backcrossing. Selection eliminates anyplants that do not have the desired gene and resistance trait, and onlythose plants that have the trait are used in the subsequent backcross.This process is then repeated for all additional backcross generations.

Selection of tomato plants for breeding is not necessarily dependent onthe phenotype of a plant and instead can be based on geneticinvestigations. For example, one can utilize a suitable genetic markerwhich is closely genetically linked to a trait of interest. One of thesemarkers can be used to identify the presence or absence of a trait inthe offspring of a particular cross, and can be used in selection ofprogeny for continued breeding. This technique is commonly referred toas marker assisted selection. Any other type of genetic marker or otherassay which is able to identify the relative presence or absence of atrait of interest in a plant can also be useful for breeding purposes.Procedures for marker assisted selection are well known in the art. Suchmethods will be of particular utility in the case of recessive traitsand variable phenotypes, or where conventional assays may be moreexpensive, time consuming or otherwise disadvantageous. Types of geneticmarkers which could be used in accordance with the invention include,but are not necessarily limited to, Simple Sequence Length Polymorphisms(SSLPs) (Williams et al., Nucleic Acids Res., 1 8:6531-6535, 1990),Randomly Amplified Polymorphic DNAs (RAPDs), DNA AmplificationFingerprinting (DAF), Sequence Characterized Amplified Regions (SCARs),Arbitrary Primed Polymerase Chain Reaction (AP-PCR), Amplified FragmentLength Polymorphisms (AFLPs) (EP 534 858, specifically incorporatedherein by reference in its entirety), and Single NucleotidePolymorphisms (SNPs) (Wang et al., Science, 280:1077-1082, 1998).

E. Plants Derived by Genetic Engineering

Many useful traits that can be introduced by backcrossing, as well asdirectly into a plant, are those which are introduced by moleculargenetic methods. Such methods include, but are not limited to, variousplant transformation techniques and methods for site-specificrecombination, the use of which are well-known in the art, and include,for example, the CRISPR-Cas system, zinc-finger nucleases (ZFNs), andtranscription activator-like effector nucleases (TALENs), among others.

In one embodiment of the invention, genetic transformation may be usedto insert a selected transgene into a plant of the invention or may,alternatively, be used for the preparation of transgenes which can beintroduced by backcrossing. Methods for the transformation of plantsthat are well-known to those of skill in the art and applicable to manycrop species include, but are not limited to, electroporation,microprojectile bombardment, Agrobacterium-mediated transformation, anddirect DNA uptake by protoplasts.

To effect transformation by electroporation, one may employ eitherfriable tissues, such as a suspension culture of cells or embryogeniccallus or alternatively one may transform immature embryos or otherorganized tissue directly. In this technique, one would partiallydegrade the cell walls of the chosen cells by exposing them topectin-degrading enzymes (pectolyases) or mechanically wound tissues ina controlled manner.

An efficient method for delivering transforming DNA segments to plantcells is microprojectile bombardment. In this method, particles arecoated with nucleic acids and delivered into cells by a propellingforce. Exemplary particles include those comprised of tungsten,platinum, and preferably, gold. For the bombardment, cells in suspensionare concentrated on filters or solid culture medium. Alternatively,immature embryos or other target cells may be arranged on solid culturemedium. The cells to be bombarded are positioned at an appropriatedistance below the macroprojectile stopping plate.

An illustrative embodiment of a method for delivering DNA into plantcells by acceleration is the Biolistics Particle Delivery System, whichcan be used to propel particles coated with DNA or cells through ascreen, such as a stainless steel or Nytex screen, onto a surfacecovered with target cells. The screen disperses the particles so thatthey are not delivered to the recipient cells in large aggregates.Microprojectile bombardment techniques are widely applicable, and may beused to transform virtually any plant species.

Agrobacterium-mediated transfer is another widely applicable system forintroducing gene loci into plant cells. An advantage of the technique isthat DNA can be introduced into whole plant tissues, thereby bypassingthe need for regeneration of an intact plant from a protoplast. ModernAgrobacterium transformation vectors are capable of replication in E.coli as well as Agrobacterium, allowing for convenient manipulations(Klee et al., Nat. Biotechnol., 3(7):637-642, 1985). Moreover, recenttechnological advances in vectors for Agrobacterium-mediated genetransfer have improved the arrangement of genes and restriction sites inthe vectors to facilitate the construction of vectors capable ofexpressing various polypeptide coding genes. The vectors described haveconvenient multi-linker regions flanked by a promoter and apolyadenylation site for direct expression of inserted polypeptidecoding genes. Additionally, Agrobacterium containing both armed anddisarmed Ti genes can be used for transformation.

In those plant strains where Agrobacterium-mediated transformation isefficient, it is the method of choice because of the facile and definednature of the gene locus transfer. The use of Agrobacterium-mediatedplant integrating vectors to introduce DNA into plant cells is wellknown in the art (Fraley et al., Nat. Biotechnol., 3:629-635, 1985; U.S.Pat. No. 5,563,055).

Transformation of plant protoplasts also can be achieved using methodsbased on calcium phosphate precipitation, polyethylene glycol treatment,electroporation, and combinations of these treatments (see, e.g.,Potrykus et al., Mol. Gen. Genet., 199:183-188, 1985; Omirulleh et al.,Plant Mol. Biol., 21(3):415-428, 1993; Fromm et al., Nature,312:791-793, 1986; Uchimiya et al., Mol. Gen. Genet., 204:204, 1986;Marcotte et al., Nature, 335:454, 1988). Transformation of plants andexpression of foreign genetic elements is exemplified in Choi et al.(Plant Cell Rep., 13:344-348, 1994) and Ellul et al. (Theor. Appl.Genet., 107:462-469, 2003).

A number of promoters have utility for plant gene expression for anygene of interest including but not limited to selectable markers,scoreable markers, genes for pest tolerance, disease resistance,nutritional enhancements and any other gene of agronomic interest.Examples of constitutive promoters useful for plant gene expressioninclude, but are not limited to, the cauliflower mosaic virus (CaMV)P-35S promoter, which confers constitutive, high-level expression inmost plant tissues (see, e.g., Odel et al., Nature, 313:810, 1985),including in monocots (see, e.g., Dekeyser et al., Plant Cell, 2:591,1990; Terada and Shimamoto, Mol. Gen. Genet., 220:389, 1990); a tandemlyduplicated version of the CaMV 35S promoter, the enhanced 35S promoter(P-e35S); the nopaline synthase promoter (An et al., Plant Physiol.,88:547, 1988); the octopine synthase promoter (Fromm et al., Plant Cell,1:977, 1989); and the figwort mosaic virus (P-FMV) promoter as describedin U.S. Pat. No. 5,378,619 and an enhanced version of the FMV promoter(P-eFMV) where the promoter sequence of P-FMV is duplicated in tandem;the cauliflower mosaic virus 19S promoter; a sugarcane bacilliform viruspromoter; a commelina yellow mottle virus promoter; and other plant DNAvirus promoters known to express in plant cells.

A variety of plant gene promoters that are regulated in response toenvironmental, hormonal, chemical, and/or developmental signals can alsobe used for expression of an operably linked gene in plant cells,including promoters regulated by (1) heat (Callis et al., PlantPhysiol., 88:965, 1988), (2) light (e.g., pea rbcS-3A promoter,Kuhlemeier et al., Plant Cell, 1:471, 1989; maize rbcS promoter,Schaffner and Sheen, Plant Cell, 3:997, 1991; or chlorophyll a/b-bindingprotein promoter, Simpson et al., EMBO J., 4:2723, 1985), (3) hormones,such as abscisic acid (Marcotte et al., Plant Cell, 1:969, 1989), (4)wounding (e.g., wunl, Siebertz et al., Plant Cell, 1:961, 1989); or (5)chemicals such as methyl jasmonate, salicylic acid, or Safener. It mayalso be advantageous to employ organ-specific promoters (e.g., Roshal etal., EMBO J., 6:1155, 1987; Schernthaner et al., EMBO J., 7:1249, 1988;Bustos et al., Plant Cell, 1:839, 1989).

Exemplary nucleic acids which may be introduced to plants of thisinvention include, for example, DNA sequences or genes from anotherspecies, or even genes or sequences which originate with or are presentin the same species, but are incorporated into recipient cells bygenetic engineering methods rather than classical reproduction orbreeding techniques. However, the term “exogenous” is also intended torefer to genes that are not normally present in the cell beingtransformed, or perhaps simply not present in the form, structure, etc.,as found in the transforming DNA segment or gene, or genes which arenormally present and that one desires to express in a manner thatdiffers from the natural expression pattern, e.g., to over-express.Thus, the term “exogenous” gene or DNA is intended to refer to any geneor DNA segment that is introduced into a recipient cell, regardless ofwhether a similar gene may already be present in such a cell. The typeof DNA included in the exogenous DNA can include DNA which is alreadypresent in the plant cell, DNA from another plant, DNA from a differentorganism, or a DNA generated externally, such as a DNA sequencecontaining an antisense message of a gene, or a DNA sequence encoding asynthetic or modified version of a gene.

Many hundreds if not thousands of different genes are known and couldpotentially be introduced into a tomato plant according to theinvention. Non-limiting examples of particular genes and correspondingphenotypes one may choose to introduce into a tomato plant include oneor more genes for insect tolerance, such as a Bacillus thuringiensis(B.t.) gene, pest tolerance such as genes for fungal disease control,herbicide tolerance such as genes conferring glyphosate tolerance, andgenes for quality improvements such as yield, nutritional enhancements,environmental or stress tolerances, or any desirable changes in plantphysiology, growth, development, morphology or plant product(s). Forexample, structural genes would include any gene that confers insecttolerance including but not limited to a Bacillus insect control proteingene as described in WO 99/31248, herein incorporated by reference inits entirety, U.S. Pat. No. 5,689,052, herein incorporated by referencein its entirety, U.S. Pat. Nos. 5,500,365 and 5,880,275, hereinincorporated by reference in their entirety. In another embodiment, thestructural gene can confer tolerance to the herbicide glyphosate asconferred by genes including, but not limited to Agrobacterium strainCP4 glyphosate resistant EPSPS gene (aroA:CP4) as described in U.S. Pat.No. 5,633,435, herein incorporated by reference in its entirety, orglyphosate oxidoreductase gene (GOX) as described in U.S. Pat. No.5,463,175, herein incorporated by reference in its entirety.

Alternatively, the DNA coding sequences can affect these phenotypes byencoding a non-translatable RNA molecule that causes the targetedinhibition of expression of an endogenous gene, for example viaantisense- or cosuppression-mediated mechanisms (see, for example, Birdet al., Biotech. Gen. Engin. Rev., 9:207, 1991). The RNA could also be acatalytic RNA molecule (i.e., a ribozyme) engineered to cleave a desiredendogenous mRNA product (see for example, Gibson and Shillito, Mol.Biotech., 7:125,1997). Thus, any gene which produces a protein or mRNAwhich expresses a phenotype or morphology change of interest is usefulfor the practice of the present invention.

F. Definitions

In the description and tables herein, a number of terms are used. Inorder to provide a clear and consistent understanding of thespecification and claims, the following definitions are provided:

Allele: Any of one or more alternative forms of a gene locus, all ofwhich alleles relate to one trait or characteristic. In a diploid cellor organism, the two alleles of a given gene occupy corresponding locion a pair of homologous chromosomes.

Backcrossing: A process in which a breeder repeatedly crosses hybridprogeny, for example a first generation hybrid (F₁), back to one of theparents of the hybrid progeny. Backcrossing can be used to introduce oneor more single locus conversions from one genetic background intoanother.

Crossing: The mating of two parent plants.

Cross-Pollination: Fertilization by the union of two gametes fromdifferent plants.

Diploid: A cell or organism having two sets of chromosomes.

Emasculate: The removal of plant male sex organs or the inactivation ofthe organs with a cytoplasmic or nuclear genetic factor or a chemicalagent conferring male sterility.

Enzymes: Molecules which can act as catalysts in biological reactions.

F₁ Hybrid: The first generation progeny of the cross of two nonisogenicplants.

Genotype: The genetic constitution of a cell or organism.

Haploid: A cell or organism having one set of the two sets ofchromosomes in a diploid.

Linkage: A phenomenon wherein alleles on the same chromosome tend tosegregate together more often than expected by chance if theirtransmission was independent.

Marker: A readily detectable phenotype, preferably inherited incodominant fashion (both alleles at a locus in a diploid heterozygoteare readily detectable), with no environmental variance component, i.e.,heritability of 1.

Phenotype: The detectable characteristics of a cell or organism, whichcharacteristics are the manifestation of gene expression.

Quantitative Trait Loci (QTL): Quantitative trait loci (QTL) refer togenetic loci that control to some degree numerically representabletraits that are usually continuously distributed.

Resistance: As used herein, the terms “resistance” and “tolerance” areused interchangeably to describe plants that show no symptoms to aspecified biotic pest, pathogen, abiotic influence or environmentalcondition. These terms are also used to describe plants showing somesymptoms but that are still able to produce marketable product with anacceptable yield. Some plants that are referred to as resistant ortolerant are only so in the sense that they may still produce a crop,even though the plants are stunted and the yield is reduced.

Regeneration: The development of a plant from tissue culture.

Royal Horticultural Society (RHS) Color Chart Value: The RHS color chartis a standardized reference which allows accurate identification of anycolor. A color's designation on the chart describes its hue, brightnessand saturation. A color is precisely named by the RHS color chart byidentifying the group name, sheet number and letter, e.g., Yellow-OrangeGroup 19A or Red Group 41B.

Self-Pollination: The transfer of pollen from the anther to the stigmaof the same plant.

Single Locus Converted (Conversion) Plant: Plants which are developed bya plant breeding technique called backcrossing, wherein essentially allof the morphological and physiological characteristics of a tomatovariety are recovered in addition to the characteristics of the singlelocus transferred into the variety via the backcrossing technique and/orby genetic transformation.

Substantially Equivalent: A characteristic that, when compared, does notshow a statistically significant difference (e.g., p=0.05) from themean.

Tissue Culture: A composition comprising isolated cells of the same or adifferent type or a collection of such cells organized into parts of aplant.

Transgene: A genetic locus comprising a sequence which has beenintroduced into the genome of a tomato plant by transformation or sitespecific recombination.

G. Deposit Information

A deposit of tomato hybrid SVTD0140 and inbred parent lines FDR9Q14-0260and FDR-9Q10189, disclosed above and recited in the claims, has beenmade with the American Type Culture Collection (ATCC), 10801 UniversityBlvd., Manassas, Va. 20110-2209. The dates of deposit for tomato hybridSVTD0140 and inbred parent lines FDR9Q14-0260 and FDR-9Q10189 were Aug.4, 2017, Jun. 13, 2017, and Jun. 13, 2017, respectively. The accessionnumbers for those deposited seeds of tomato hybrid SVTD0140 and inbredparent lines FDR9Q14-0260 and FDR-9Q10189 are ATCC Accession NumberPTA-124391, ATCC Accession Number PTA-124249, and ATCC Accession NumberPTA-124250, respectively. Upon issuance of a patent, all restrictionsupon the deposits will be removed, and the deposits are intended to meetall of the requirements of 37 C.F.R. § 1.801-1.809. The deposits will bemaintained in the depository for a period of 30 years, or 5 years afterthe last request, or for the effective life of the patent, whichever islonger, and will be replaced if necessary during that period.

Although the foregoing invention has been described in some detail byway of illustration and example for purposes of clarity andunderstanding, it will be obvious that certain changes and modificationsmay be practiced within the scope of the invention, as limited only bythe scope of the appended claims.

All references cited herein are hereby expressly incorporated herein byreference.

What is claimed:
 1. A tomato plant comprising at least a first set ofthe chromosomes of tomato line FDR-9Q10189, a sample of seed of saidline having been deposited under ATCC Accession Number PTA-124250.
 2. Atomato seed that produces the plant of claim
 1. 3. A plant part of theplant of claim 1, wherein the plant part comprises a cell of said plant.4. A tomato plant having all the physiological and morphologicalcharacteristics of the plant of claim
 1. 5. A tissue culture ofregenerable cells of the plant of claim
 1. 6. A method of vegetativelypropagating the tomato plant of claim 1, the method comprising the stepsof: (a) collecting tissue capable of being propagated from the plantaccording to claim 1; and (b) propagating a tomato plant from saidtissue.
 7. A method of introducing a trait into a tomato line, themethod comprising: (a) utilizing as a recurrent parent the plant ofclaim 1 by crossing said plant with a donor tomato plant that comprisesa trait to produce F₁ progeny; (b) selecting an F₁ progeny thatcomprises the trait; (c) backcrossing the selected F₁ progeny with aplant of the same tomato line used as the recurrent parent in step (a)to produce backcross progeny; (d) selecting a backcross progenycomprising the trait and the morphological and physiologicalcharacteristics of the recurrent parent tomato line used in step (a);and (e) repeating steps (c) and (d) three or more times to produce aselected fourth or higher backcross progeny.
 8. A tomato plant producedby the method of claim 7, wherein said plant comprises the trait andotherwise comprises all of the physiological and morphologicalcharacteristics of tomato line FDR-9Q10189.
 9. A method of producing atomato plant comprising an added trait, the method comprisingintroducing a transgene by genetic transformation or site-specificmodification conferring the trait into the plant of claim
 1. 10. Atomato plant produced by the method of claim
 9. 11. A tomato plantcomprising at least a first set of the chromosomes of tomato lineFDR-9Q10189, a sample of seed of said line having been deposited underATCC Accession Number PTA-124250, further comprising a transgene. 12.The plant of claim 11, wherein the transgene confers a trait selectedfrom the group consisting of male sterility, herbicide tolerance, insectresistance, pest resistance, disease resistance, modified fatty acidmetabolism, environmental stress tolerance, modified carbohydratemetabolism, and modified protein metabolism.
 13. A tomato plantcomprising at least a first set of the chromosomes of tomato lineFDR-9Q10189, a sample of seed of said line having been deposited underATCC Accession Number PTA-124250, further comprising a single locusconversion.
 14. The plant of claim 13, wherein the single locusconversion confers a trait selected from the group consisting of malesterility, herbicide tolerance, insect resistance, pest resistance,disease resistance, modified fatty acid metabolism, environmental stresstolerance, modified carbohydrate metabolism, and modified proteinmetabolism.
 15. A method for producing a seed of a tomato plant derivedfrom tomato line FDR-9Q10189, the method comprising the steps of: (a)crossing a tomato plant according to claim 1 with itself or a secondtomato plant; and (b) allowing seed of a line FDR-9Q10189-derived tomatoplant to form.
 16. A method of producing a seed of a lineFDR-9Q10189-derived tomato plant, the method comprising the steps of:(a) producing a line FDR-9Q10189-derived tomato plant from a seedproduced by crossing a tomato plant according to claim 1 with itself ora second tomato plant; and (b) crossing the line FDR-9Q10189-derivedtomato plant with itself or a different tomato plant to obtain a seed ofa line FDR-9Q10189-derived tomato plant.
 17. The method of claim 16, themethod further comprising producing a tomato plant grown from the seedof said step (b) and crossing said tomato plant with itself or adifferent tomato plant to produce a seed of a further lineFDR-9Q10189-derived tomato plant.
 18. A method of producing a tomatofruit, the method comprising: (a) obtaining the plant according to claim1, wherein the plant has been cultivated to maturity; and (b) collectinga tomato fruit from the plant.
 19. The plant of claim 1, wherein theplant is a plant of said tomato line FDR-9Q10189.
 20. The seed of claim2, wherein the seed is a seed of said tomato line FDR-9Q10189.